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核酸适配体——从体外筛选到体内应用

Nucleic acid aptamers-from selection in vitro to applications in vivo.

作者信息

Famulok M, Mayer G, Blind M

机构信息

Kekulé-Institut für Organische Chemie und Biochemie, Gerhard Domagk-Strasse 1, 53121 Bonn, Germany.

出版信息

Acc Chem Res. 2000 Sep;33(9):591-9. doi: 10.1021/ar960167q.

Abstract

Aptamers are nucleic acid ligands which are isolated from combinatorial oligonucleotide libraries by in vitro selection. They exhibit highly complex and sophisticated molecular recognition properties and are capable of binding tightly and specifically to targets ranging from small molecules to complex multimeric structures. Besides their promising application as molecular sensors, many aptamers targeted against proteins are also able to interfere with the proteins' biological function. Recently developed techniques facilitate the intracellular application of aptamers and their use as in vivo modulators of cellular physiology. Using these approaches, one can quickly obtain highly specific research reagents that act on defined intracellular targets in the context of the living cell.

摘要

适体是通过体外筛选从组合寡核苷酸文库中分离出来的核酸配体。它们具有高度复杂和精细的分子识别特性,能够紧密且特异性地结合从小分子到复杂多聚体结构的各种靶标。除了作为分子传感器具有广阔的应用前景外,许多针对蛋白质的适体还能够干扰蛋白质的生物学功能。最近开发的技术促进了适体在细胞内的应用及其作为细胞生理体内调节剂的用途。使用这些方法,可以快速获得作用于活细胞内特定细胞靶点的高度特异性研究试剂。

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